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Annals of the Rheumatic Diseases logoLink to Annals of the Rheumatic Diseases
. 1993 Jun;52(6):449–453. doi: 10.1136/ard.52.6.449

Microfibrillar elements in the synovial joint: presence of type VI collagen and fibrillin-containing microfibrils.

A D Waggett 1, C M Kielty 1, C A Shuttleworth 1
PMCID: PMC1005070  PMID: 8323397

Abstract

OBJECTIVES--The aims were to isolate and positively identify the microfibrillar elements which have been observed in the synovial lining. In addition, synovial fluid was examined for these elements to improve the understanding of the role of these structures in health and disease. METHODS--Bacterial collagenase digestion of bovine synovial linings and human and bovine synovial fluids was used to release intact, non-denatured microfibrillar elements. The microfibrils were isolated by Sepharose CL-2B chromatography and viewed by rotary shadowing. They were characterised by immunogold labelling with specific antibodies. RESULTS--Intact type VI collagen microfibrils and fibrillin-containing microfibrils were isolated and positively identified in the synovial lining from bovine ankle joints by immunogold labelling. Type VI collagen microfibrils were also present in the synovial fluid. CONCLUSIONS--The role of the microfibrillar elements in vivo is not fully understood, but their distribution in the synovial lining suggests they have an important role in the mechanical and physical properties of this tissue. The presence of type VI collagen microfibrils in synovial fluid poses the intriguing possibility that it may represent a product of microfibril turnover and a potential early marker for rheumatoid arthritis. Alternatively, type VI collagen may be specifically secreted into the synovial fluid to interact with hyaluronan and form part of the structure of synovial fluid.

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Selected References

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  1. Ashhurst D. E., Bland Y. S., Levick J. R. An immunohistochemical study of the collagens of rabbit synovial interstitium. J Rheumatol. 1991 Nov;18(11):1669–1672. [PubMed] [Google Scholar]
  2. CASTOR C. W., MUIRDEN K. D. COLLAGEN FORMATION IN MONOLAYER CULTURES OF HUMAN FIBROBLASTS. THE EFFECTS OF HYDROCORTISONE. Lab Invest. 1964 Jun;13:560–574. [PubMed] [Google Scholar]
  3. Castor C. W., Roberts D. J., Hossler P. A., Bignall M. C. Connective tissue activation. XXV. Regulation of proteoglycan synthesis in human synovial cells. Arthritis Rheum. 1983 Apr;26(4):522–527. doi: 10.1002/art.1780260411. [DOI] [PubMed] [Google Scholar]
  4. Engvall E., Hessle H., Klier G. Molecular assembly, secretion, and matrix deposition of type VI collagen. J Cell Biol. 1986 Mar;102(3):703–710. doi: 10.1083/jcb.102.3.703. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Fife R. S., Myers S. L. Evidence for an interaction between canine synovial cell proteoglycans and link proteins. Biochim Biophys Acta. 1985 Dec 13;843(3):238–244. doi: 10.1016/0304-4165(85)90144-8. [DOI] [PubMed] [Google Scholar]
  6. HAMERMAN D., RUSKIN J. Histologic studies on human synovial membrane. I. Metachromatic staining and the effects of streptococcal hyaluronidase. Arthritis Rheum. 1959 Dec;2:546–552. doi: 10.1002/1529-0131(195912)2:6<546::aid-art1780020609>3.0.co;2-l. [DOI] [PubMed] [Google Scholar]
  7. Keene D. R., Maddox B. K., Kuo H. J., Sakai L. Y., Glanville R. W. Extraction of extendable beaded structures and their identification as fibrillin-containing extracellular matrix microfibrils. J Histochem Cytochem. 1991 Apr;39(4):441–449. doi: 10.1177/39.4.2005373. [DOI] [PubMed] [Google Scholar]
  8. Kielty C. M., Cummings C., Whittaker S. P., Shuttleworth C. A., Grant M. E. Isolation and ultrastructural analysis of microfibrillar structures from foetal bovine elastic tissues. Relative abundance and supramolecular architecture of type VI collagen assemblies and fibrillin. J Cell Sci. 1991 Aug;99(Pt 4):797–807. doi: 10.1242/jcs.99.4.797. [DOI] [PubMed] [Google Scholar]
  9. Kielty C. M., Whittaker S. P., Grant M. E., Shuttleworth C. A. Attachment of human vascular smooth muscles cells to intact microfibrillar assemblies of collagen VI and fibrillin. J Cell Sci. 1992 Oct;103(Pt 2):445–451. doi: 10.1242/jcs.103.2.445. [DOI] [PubMed] [Google Scholar]
  10. Kielty C. M., Whittaker S. P., Grant M. E., Shuttleworth C. A. Type VI collagen microfibrils: evidence for a structural association with hyaluronan. J Cell Biol. 1992 Aug;118(4):979–990. doi: 10.1083/jcb.118.4.979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Levick J. R., McDonald J. N. Microfibrillar meshwork of the synovial lining and associated broad banded collagen: a clue to identity. Ann Rheum Dis. 1990 Jan;49(1):31–36. doi: 10.1136/ard.49.1.31. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Levick J. R. Permeability of rheumatoid and normal human synovium to specific plasma proteins. Arthritis Rheum. 1981 Dec;24(12):1550–1560. doi: 10.1002/art.1780241215. [DOI] [PubMed] [Google Scholar]
  13. Linck G., Porte A. B-cells of the synovial membrane. III. Relationship with the specific collagenous structure of the intimal interstitium in the mouse. Cell Tissue Res. 1981;218(1):117–121. doi: 10.1007/BF00210097. [DOI] [PubMed] [Google Scholar]
  14. Linck G., Stocker S., Grimaud J. A., Porte A. Distribution of immunoreactive fibronectin and collagen (type I, III, IV) in mouse joints. Fibronectin, an essential component of the synovial cavity border. Histochemistry. 1983;77(3):323–328. doi: 10.1007/BF00490895. [DOI] [PubMed] [Google Scholar]
  15. Mapp P. I., Revell P. A. Fibronectin production by synovial intimal cells. Rheumatol Int. 1985;5(5):229–237. doi: 10.1007/BF00541341. [DOI] [PubMed] [Google Scholar]
  16. Mould A. P., Holmes D. F., Kadler K. E., Chapman J. A. Mica sandwich technique for preparing macromolecules for rotary shadowing. J Ultrastruct Res. 1985 Apr;91(1):66–76. doi: 10.1016/0889-1605(85)90077-1. [DOI] [PubMed] [Google Scholar]
  17. Okada Y., Nakanishi I., Kajikawa K. Ultrastructure of the mouse synovial membrane. Development and organization of the extracellular matrix. Arthritis Rheum. 1981 Jun;24(6):835–843. doi: 10.1002/art.1780240611. [DOI] [PubMed] [Google Scholar]
  18. Pollock L. E., Lalor P., Revell P. A. Type IV collagen and laminin in the synovial intimal layer: an immunohistochemical study. Rheumatol Int. 1990;9(6):277–280. doi: 10.1007/BF00541324. [DOI] [PubMed] [Google Scholar]
  19. Roy S., Ghadially F. N. Synthesis of hyaluronic acid by synovial cells. J Pathol Bacteriol. 1967 Apr;93(2):555–557. doi: 10.1002/path.1700930216. [DOI] [PubMed] [Google Scholar]
  20. Sheehan J. K., Oates K., Carlstedt I. Electron microscopy of cervical, gastric and bronchial mucus glycoproteins. Biochem J. 1986 Oct 1;239(1):147–153. doi: 10.1042/bj2390147. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Shuttleworth C. A., Berry L., Kielty C. M. Microfibrillar components in dental pulp: presence of both type VI collagen- and fibrillin-containing microfibrils. Arch Oral Biol. 1992 Dec;37(12):1079–1084. doi: 10.1016/0003-9969(92)90040-f. [DOI] [PubMed] [Google Scholar]

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